Reaction Details |
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Target | P2Y purinoceptor 1 |
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Ligand | BDBM50184371 |
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Substrate/Competitor | n/a |
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Meas. Tech. | ChEMBL_805341 (CHEMBL1955234) |
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EC50 | 900±n/a nM |
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Citation | Yelovitch, S; Camden, J; Weisman, GA; Fischer, B Boranophosphate isoster controls P2Y-receptor subtype selectivity and metabolic stability of dinucleoside polyphosphate analogues. J Med Chem55:437-48 (2012) [PubMed] Article |
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More Info.: | Get all data from this article, Assay Method |
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P2Y purinoceptor 1 |
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Name: | P2Y purinoceptor 1 |
Synonyms: | P2RY1 | P2RY1_MELGA |
Type: | n/a |
Mol. Mass.: | 41199.64 |
Organism: | Meleagris gallopavo |
Description: | n/a |
Residue: | 362 |
Sequence: | MTEALISAALNGTQPELLAGGWAAGNASTKCSLTKTGFQFYYLPTVYILVFITGFLGNSV
AIWMFVFHMRPWSGISVYMFNLALADFLYVLTLPALIFYYFNKTDWIFGDVMCKLQRFIF
HVNLYGSILFLTCISVHRYTGVVHPLKSLGRLKKKNAVYVSSLVWALVVAVIAPILFYSG
TGVRRNKTITCYDTTADEYLRSYFVYSMCTTVFMFCIPFIVILGCYGLIVKALIYKDLDN
SPLRRKSIYLVIIVLTVFAVSYLPFHVMKTLNLRARLDFQTPQMCAFNDKVYATYQVTRG
LASLNSCVDPILYFLAGDTFRRRLSRATRKSSRRSEPNVQSKSEEMTLNILTEYKQNGDT
SL
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BDBM50184371 |
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n/a |
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Name | BDBM50184371 |
Synonyms: | CHEMBL218604 | [bis({[(2R,3S,4R,5R)-5-(6-amino-9H-purin-9-yl)-3,4-dihydroxyoxolan-2-yl]methyl phosphonato}oxy)phosphoryl]boranuide; tris(tributylamine) |
Type | Small organic molecule |
Emp. Form. | C20H27BN10O15P3 |
Mol. Mass. | 751.22 |
SMILES | [BH3-]P(=O)(OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12)OP([O-])(=O)OC[C@H]1O[C@H]([C@H](O)[C@@H]1O)n1cnc2c(N)ncnc12 |
Structure |
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